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Dressers sold on Walmart.com recalled for tip-over hazard
The furniture violates federal safety regulations
March 24, 2025About 28,590 GIKPAL dressers are being recalled because they can tip over on young children. The dressers were sold exclusively on Walmart.com by ONME Direct.
The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate the performance and labeling requirements of the STURDY Act.
This recall involves GIKPAL 10 drawer dressers with model number HI1318_13. The dressers were sold in rustic brown with black handles and black sides and back. The dressers measure about 11.8 inches wide, 38.9 inches long and 39.4 inches tall, and weigh about 36 pounds. The model number HI1318_13, Fabric Dresser and Made in China are printed on the product packaging.
What to do
Consumers should immediately stop using the recalled dressers if they are not properly anchored to a wall and place them in an area that children cannot access. Contact ONME Direct for instructions to receive a full refund and submit a photo of the consumer disposing of the product to onmeus@outlook.com. ONME Direct and Walmart are contacting all known purchasers directly.
Consumers may contact ONME Direct toll-free at 833-449-5777 from 9 a.m. to 6 p.m. PT Monday through Friday, email at onmeus@outlook.com, or online at https://onmeus.com/pages/recall-1 or https://onmeus.com and click Recall at the top of the page for more information.
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Segway Ninebot Max G30P and Max G30LP KickScooters recalled due to fall hazard
The company has received reports of 20 injuries
March 21, 2025Segway has issued a recall for 220,000 Segway Ninebot Max G30P and Max G30LP KickScooters because The folding mechanism can fail and cause the handlebars or stem to fold while the scooter is in use, posing a fall hazard to riders.
Segway has received 68 reports of folding mechanism failures, including 20 injuries to include abrasions, bruises, lacerations and broken bones. The scooters were sold at Best Buy, Costco, Walmart, Target and Sams Club nationwide and online at Segway.com and Amazon.com from January 2020 through February 2025 for between $600 and $1,000.
This recall involves all Segway Ninebot Max G30P and Max G30LP KickScooters. The Max G30LP KickScooter is gray in color with yellow accents and the Max G30P is black in color with yellow accents.
The brand name ninebot appears on the foot platform and the top of the handlebars. The model number is located on a label on the side of the foot deck. The Max G30P model is 46 inches long, 19 inches wide, 47 inches high and weighs 42 pounds. The Max G30LP model is 44 inches long, 19 inches wide, 45 inches high and weighs 39 pounds.
What to do
Consumers should immediately stop using the recalled scooters and contact Segway to receive information to determine whether the folding mechanism needs adjustment and to receive a free maintenance kit. The kit includes tools and instructions for checking and tightening the folding mechanism and keeping it properly maintained.
Consumers may contact Segway at 800-914-6110 from 9 a.m. to 5 p.m. Monday through Friday, email at recall@segway.com, or online at https://service.segway.com/recall or www.segway.com, and click on Recall Center at the bottom of the page for more information.
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Espresso machines recalled due to burn and laceration hazards
The manufacturer has received eight reports of injuries
March 20, 2025Sensio has issued a recall for about 12,300 steam espresso machines due to burn and laceration hazards. The brew cup handle can forcefully eject during use, shattering the glass carafe and posing a burn and laceration hazard.
The firm has received 18 reports of the handles ejecting, eight of which reported burn and/or laceration injuries. The machines were sold at JCPenney stores nationwide and online at BestBuy.com and JCPenney.com from August 2023 through January 2025 for between $40 and $60.
This recall involves the Bella Pro Series Steam Espresso Maker, Model 90195 and Cooks Steam Espresso Makers, Model 22395. The recalled espresso machines are black with stainless steel trim and measure about six inches wide and 12 inches high. The machines have Bella Pro Series or Cooks on the steaming chamber and the model number is identified as the Item number on a sticker under the machine.
What to do
Consumers should immediately stop using the recalled espresso machines and contact Sensio for a refund.
Contact Sensio toll-free at 855-647-3125 from 8 a.m. to 5 p.m. ET Monday through Friday or online at www.bellakitchenware.com and click on Recalls for more information.
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Popular acne products recalled due to high benzene levels
While the majority of products have safe levels of the chemical, its important for consumers to know the risks
March 19, 2025The Food and Drug Administration (FDA) has announced the voluntary recall of several popular acne products due to high levels of benzene.
The chemical is used in the production of products like dyes, detergents, and some plastics, and its also emitted into the air by cigarette smoke. However, exposure to benzene comes with health risks.
The health consequences of benzene exposure depend on the amount, route, and length of time of exposure, as well as age and preexisting medical conditions of the product user, the FDA explained.
In small amounts over long periods of time, benzene can decrease the formation of blood cells. Long-term exposure to benzene through inhalation, oral intake, and skin absorption may result in cancers such as leukemia and other blood disorders.
What products are recalled?
The FDA conducted independent testing of nearly 100 popular acne products to determine the levels of benzene of products currently on store shelves.
While over 90% of the products tested were safe, there were some products with benzoyl peroxide that translated to unsafe levels of benzene.
Heres a look at the affected products:
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La Roche-Posay Effaclar Duo Dual Action Acne Treatment
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Lot Number: MYX46W
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Expiration Date: April 2025
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Walgreens Acne Control Cleanser
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Lot Number: 23 09328
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Expiration Date: September 2025
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Proactiv Emergency Blemish Relief Cream Benzoyl Peroxide 5%
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Lot Number: V3305A; V3304A
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Expiration Date: October 2025
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Proactiv Skin Smoothing Exfoliator
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Lot Number: V4204A
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Expiration Date: July 2025
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SLMD Benzoyl Peroxide Acne Lotion
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Lot Number: 2430600
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Expiration Date: March 2025
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Walgreens Tinted Acne Treatment Cream
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Lot Number: 49707430
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Expiration Date: March 2026
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Another product to look out for is Zapzyt Acne Treatment Gel. The manufacturer issued its own voluntary recall of the product due to high benzene levels, independent of the FDAs investigation.
At this time, this recall is directed to retailers, meaning these products should be removed from store shelves. However, the FDA doesnt have any specific instructions for consumers discontinuing personal use.
It is important to note that the FDA encourages consumers to diligently check the expiration dates on all of their skincare products and dispose of any that have expired.
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Lean Cuisine, Stouffer's frozen meals recalled
They may contain a wood-like contaminant that could cause choking
March 18, 2025Nestl USA has issued a voluntary recall for select batches of Lean Cuisine and STOUFFER'S frozen meals due to a potential contamination with wood-like material. The recall was prompted by a consumer report of a possible choking incident, and the company is collaborating with the U.S. Food & Drug Administration (FDA) and the U.S. Department of Agriculture (USDA).
The recalled products were produced between August 2024 and March 2025 and distributed to major retailers across the United States from September 2024 to March 2025. At this time, the total number of affected units has not been publicly released. Nestl USA has removed the products from sale and is offering refunds or replacements.
What to look for?
Product name and description:
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Lean Cuisine Butternut Squash Ravioli
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Lean Cuisine Spinach Artichoke Ravioli
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Lean Cuisine Lemon Garlic Shrimp Stir Fry
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STOUFFER'S Party Size Chicken Lasagna (96oz)
All items are frozen meals packaged in boxes or trays bearing the Lean Cuisine or STOUFFER'S brand name.
Identifiers:
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The lot numbers and best-before dates are printed on the product packaging
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Affected Lean Cuisine codes include: 4261595912 (OCT2025), 4283595912 (NOV2025), 4356595912 (JAN2026), 5018595912 (FEB2026), 5038595912 (MAR2026), and 4214595511 (SEPT2025)
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Affected STOUFFER'S codes include: 4262595915 (OCT2025), 4351595915 (JAN2026), 5051595915 (MAR2026), 5052595915 (MAR2026)
Affected purchase locations and dates:
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Distributed to major retailers throughout the United States
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Sold between September 2024 and March 2025
What should buyers do?
Product handling:
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Do not consume the affected meals
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Return them to the place of purchase for a full refund or replacement
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If discarding, follow local waste guidelines
Refunds, replacements, or repairs:
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Contact Nestl USA at (800) 681-1676 for information on refunds or replacements
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Phone lines are open MondayFriday, 9 AM6 PM EST
Health and safety advice:
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If anyone has experienced symptoms such as gagging or choking after consuming these meals, consider seeking medical attention
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Watch for continued breathing difficulty or persistent throat irritation
Sources
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Gerolsteiner recalls sparkling water bottles from Trader Joe’s due to laceration risk
Glass bottle cracking prompts recall of Gerolsteiner water from Trader Joe's
March 14, 2025Gerolsteiner has initiated a voluntary recall of its 750ml Sparkling Natural Mineral Water sold under specific lot numbers. The recall addresses a potential laceration hazard associated with cracking glass bottles.
These products were distributed through Trader Joes stores across 12 states (Alabama, Arkansas, Colorado, Florida, Georgia, Kansas, Louisiana, New Mexico, Oklahoma, South Carolina, Tennessee, and Texas). Approximately 61,500 bottles are affected. Gerolsteiner is working with authorities and has removed the products from store shelves.
What to look for?
Product name and description:
- Gerolsteiner Sparkling Natural Mineral Water (750ml glass bottles)
- White, blue, and red label featuring Gerolsteiner branding
Identifiers:
- Lot numbers: 11/28/2024 L or 11/27/2024 L
- Lot information printed on the lower part of the label
Affected purchase locations and dates:
- Sold at Trader Joes in Alabama, Arkansas, Colorado, Florida, Georgia, Kansas, Louisiana, New Mexico, Oklahoma, South Carolina, Tennessee, and Texas
- Purchased between December 2024 and January 2025
What should buyers do?
Handling the product:
- Stop using and do not consume the affected water
- Return bottles to the place of purchase for a refund
Refunds, replacements, or repairs:
- Contact Gerolsteiners customer service at 800-777-0633 (available MondayFriday, 8:30 AM5 PM ET) or email customerservice@consup.us for more information
- A refund is provided upon return of the product
Health and safety advice:
- No injuries have been reported. If any lacerations occur, seek medical attention as needed
Sources
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Dr. Reddy’s recalls levetiracetam infusion bags nationwide due to mislabeling
Nationwide recall due to double dose risk from mislabeled infusion bags
March 13, 2025Dr. Reddys Laboratories has initiated a voluntary recall of Levetiracetam in 0.75% Sodium Chloride Injection (1,000 mg/100 mL), identified as Lot Number A1540076. The issue involves mislabeling of infusion bags that were incorrectly marked as containing 500 mg/100 mL of the medication rather than 1,000 mg/100 mL.
This discrepancy may lead to the administration of double the intended dose. The problem was identified after distribution, prompting a nationwide recall. The affected infusion bags were shipped between November 4 and November 6, 2024, through hospitals, pharmacies, and distributors across the United States. The company has not reported any adverse events at this time. As part of the recall, the product is being removed from circulation, and replacements or refunds are being offered to impacted purchasers.
What to look for?
Product name and description:
- Levetiracetam in 0.75% Sodium Chloride Injection (1,000 mg/100 mL)
- Packaged in infusion bags labeled incorrectly as Levetiracetam in 0.82% Sodium Chloride Injection (500 mg/100 mL)
Identifiers:
- Lot Number: A1540076
- The lot number is printed on the infusion bags label
- Correct strength is 1,000 mg/100 mL, despite the 500 mg/100 mL labeling
Affected purchase locations and dates:
- Distributed nationwide through hospitals, pharmacies, and medical distributors
- Shipped from November 4, 2024, through November 6, 2024
What should buyers do?
Product handling:
- Return the affected infusion bags to the original purchase source or follow the instructions provided by Dr. Reddys Laboratories
- Do not administer the mislabeled product under any circumstance
Refunds, replacements, or repairs:
- Contact Inmar for a prepaid return label or refund at 1-877-645-1584
- Customer service is available Monday through Friday from 9 AM to 5 PM EST
Health and safety advice:
- Seek medical attention if you believe you or someone under your care has received the mislabeled medication
- Watch for potential adverse effects such as dizziness, somnolence, respiratory issues, or other indications of overdose
Sources
- FDA recall notice
- Business Wire announcement
- CNBC TV18 coverage
- Stock Titan notice
- NDTV Profit article
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Retractable safety gates recalled due to child entrapment hazard
Safety gates recalled after tests reveal child entrapment risk
March 13, 2025A recall has been issued for retractable safety mesh gates marketed for child or pet use under model number SG021. The recall is being conducted in coordination with the U.S. Consumer Product Safety Commission.
The entrapment hazard was identified when safety testing revealed that a childs torso could fit through the opening between the gate and the floor. Approximately 880 units have been affected. These gates were sold on Amazon from September 2024 to January 2025. The company is removing the product from the market and offering full refunds.
What to look for?
Product name and description:
- Retractable safety gates labeled as Retractable Safety Gate with model SG021
- Colors: white, gray, and black
- Height: about 34 inches, adjustable up to around 55 inches in width
- Frame made of aluminum
- A white label inside the frame near the handles shows the product name and model
Identifiers:
- Model number SG021 printed on the label near the handles
- Look for the text Retractable Safety Gate on the gates frame
- The label with this information is placed inside the frame near the handles
Affected purchase locations and dates:
- Sold exclusively on Amazon
- Purchased between September 2024 and January 2025
What should buyers do?
Use or disposal advice:
- Stop using the recalled gate immediately
- Destroy it by cutting the mesh
- Dispose of it following local waste guidelines
Refunds, replacements, or repairs:
- A full refund is available
- Contact the company by phone at 771-232-2236 from 10 a.m. to 4 p.m. ET, Monday through Friday
- Email support at [emailprotected]
- Provide a photo of the destroyed gate to receive instructions for the refund
Health and safety advice:
- No injuries have been reported
- If a child has experienced any incident related to the recalled gate, seek medical attention for potential torso or neck injuries
- Monitor for bruising, discomfort, or trouble breathing
Sources
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BMC recalls Kaius 01 bicycles and framesets due to fall hazard
BMC recalls 10,000 bikes over risk of fork steerer tube failure
March 13, 2025A voluntary recall has been issued for all BMC Kaius 01 bicycles and framesets, including those with a V5 fork. The recall stems from a potential fall hazard caused by the fork steerer tube, which can crack or separate during use.
The issue surfaced after reports of steerers coming loose, though no injuries have been reported. About 10,000 units are affected and were distributed by BMC USA Corporation. They were sold through authorized BMC dealers across various regions. BMC is removing the products from circulation and offering free replacement forks to those affected.
What to look for?
Product name and description:
- BMC Kaius 01 bicycles and framesets
- Offered in Peacock Spider, Carbon Black/Brushed Blue, Purple/White, White/Black, Turquoise/Black, Saffron/Black, and Stone Grey
- The brand name BMC is printed on the downtube
Identifiers:
- V5 fork
- Manufacturing details found on the original label near the fork steerer tube
- Owners may locate the model name and branding on the bike frame
Affected purchase locations and dates:
- Sold through authorized BMC dealers
- Records indicate sales leading up to the recall date of March 13, 2025
What should buyers do?
Instructions for buyers:
- Stop using the recalled bicycles or framesets
- Contact an authorized BMC dealer for guidance on free inspection and fork replacement
Refunds, replacements, or repairs:
- A free fork replacement is available
- Contact the company by phone at 888-262-7755 from 9 AM to 5 PM PT, Monday through Friday
- Email kaius-fork-recall-USA@BMC-Switzerland.com for a prepaid return label if needed
- Visit the BMC website for more assistance if the purchase history is unclear
Health and safety advice:
- If anyone experiences a fork failure while riding, watch for injuries such as bruises or fractures
- Seek medical evaluation if any concerning symptoms arise from a fall or accident
Sources
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Sublue recalls black lithium-ion batteries for Mix underwater scooters due to fire hazard
Fire risk prompts recall of batteries in Sublue Mix underwater scooters
March 13, 2025Sublue has issued a voluntary recall for certain black lithium-ion batteries used in the Sublue Mix underwater scooters. The recall addresses a fire hazard associated with these batteries, which can overheat and ignite.
This issue was identified after 161 reports of thermal and swelling incidents, including eight fires, one injury, and property damage. Approximately 40,370 units are affected. The recalled batteries were sold through various retailers and online channels in the United States. Sublue is removing the affected products from circulation and providing replacement batteries at no cost to consumers.
What to look for?
Product name and description:
- Sublue Mix underwater scooter
- Available in arctic white, space blue, and aqua blue
- Sublue printed on top
- Whiteshark Mix Underwater Scooter printed on the side
- Battery compartment located on the underside of the scooter
Identifiers:
- Black lithium-ion batteries for Sublue Mix underwater scooters
- Replacement batteries for these scooters (black only)
- The batch or lot number is printed on the battery housing
Affected purchase locations and dates:
- Sold nationwide through various retailers and online vendors
- Distributed from date of product launch to the present
What should buyers do?
Product handling:
- Stop using the scooter with the recalled black battery
- Do not dispose of the recalled battery in regular trash or common battery recycling boxes
- Follow local and state guidelines for safe battery disposal
Refunds, replacements, or repairs:
- Contact Sublue for a free replacement gray battery
- Request a prepaid return label or battery collection kit by phone, email, or the company website
- Phone: 855-206-8698 (9 AM 5 PM PT, MondaySunday)
- Email: support.us@sublue.com
- Website: Sublue recall information page (also accessible via Recalls at the top of the homepage)
Health and safety advice:
- If the battery shows signs of swelling, smells unusual, or is hot to the touch, store it in a safe, ventilated area away from combustible materials
- Seek medical attention if burns or smoke inhalation occurred due to battery ignition
Sources
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Black Diamond recalls BD Vision harnesses due to potential fall hazard
Climbers urged to return faulty harnesses for refund or credit
March 13, 2025Black Diamond Equipment has announced a recall of all BD Vision Harnesses due to a potential fall hazard. This action is being carried out in coordination with the U.S. Consumer Product Safety Commission and Health Canada. The harness material may degrade over time and fail to support the climber. One report of a waist belt failure has been recorded, though no injuries have been reported. Approximately 1,580 units are affected in the United States and 130 in Canada.
The recall covers harnesses sold between January 1, 2018, and February 26, 2025, through various outdoor retailers and online channels. Black Diamond is asking consumers to stop using the product immediately and is offering refunds or store credit while working with regulators to manage the recall process.
What to look for?
Product name and description:
- BD Vision Harnesses in black and white
- Black Diamond printed on one leg loop and Vision on the other
- Fixed leg loops designed for technical alpine and ice climbing
Identifiers:
- The models name (BD Vision) is visible on the harness leg loop
- Check for the Black Diamond logo on the opposite loop
Affected purchase locations and dates:
- Sold through outdoor retailers and online stores in the U.S. and Canada
- Available for purchase between January 1, 2018, and February 26, 2025
What should buyers do?
Product handling:
- Stop using the harness immediately
- Return it to Black Diamond using a prepaid shipping label
Refunds, replacements, or repairs:
- Contact Black Diamonds customer service to receive a full refund to the original form of payment
- Opt instead for a one-time $200 credit at Black Diamond stores or website
- Customer service is available by phone at 866-306-0865 (Monday-Friday, 9 AM - 4:30 PM MT)
- Inquiries can also be sent to VisionHarnessRecall@bdel.com
Health and safety advice:
- No injuries have been reported, but a failure may cause a serious fall
- If you have used this harness and are concerned about potential injury, seek medical guidance
Sources
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Onasti Toddler Tower Stools recalled after serious injury to a child
The product was sold exclusively on Amazon by Blissful-Time
March 13, 2025Blissful-Time is recalling more than 10,000 Onasti Toddler Tower Stools because the stools can collapse or tip over while in use, posing serious fall and injury hazards to children. Blissful-Time has received four reports of the stool collapsing or tipping over, including two injuries, with one causing bruising and the other a brain injury to a toddler.
The product was sold on Amazon.com from March 2024 through December 2024 for between $72 and $90.
This recall involves Onasti-branded toddler stools. The plastic, foldable, triangular-shaped tower stools were sold in beige/white, blue/gray, green, gray/white, light blue and pink.
They measure about 25 inches long, 24 inches wide and 32 inches tall, and have handles and an adjustable platform that can be raised or lowered from two to three steps. The Onasti logo appears on the warning label on the side of the stools.
What to do
Consumers should stop using the recalled stools and store them away from children until repaired. Contact Blissful-Time to receive a free repair kit, including shipping. The repair kit consists of two steps, one base, and one guardrail. Blissful-Time is contacting all known purchasers directly.
Consumers may contact Blissful-Time toll-free at 833-999-9327, email support@onasti.net, or online at https://onasti.com/pages/product-recall-information or https://onasti.com/ and click Product Recall Information for more information.
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Kawasaki is recalling nearly 4,000 motorcycles
The clutch release shaft was not properly welded
March 12, 2025Kawasaki Motor Corp., U.S.A. (KMC) is recalling 3,742 2024 Ninja 500, Z500 ABS, and Z500 SE ABS motorcycles. The clutch release shaft was not properly welded, which can cause the clutch lever to break apart.
A broken clutch release lever may not disengage, disabling the motorcycle and increasing the risk of a crash.
What to do
Dealers will replace the clutch release shaft, free of charge. Owner notification letters are expected to be mailed March 24, 2025. Owners may contact KMC customer service at 1-866-802-9381. KMC's number for this recall is MC25-04.
Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 888-327-4236 (TTY 888-275-9171) or go to nhtsa.gov.
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Zaarah supplements recalled due to potential arsenic contamination
The products were sold in New York, New Jersey, Connecticut and California
March 11, 2025New York Wholesale Group is recalling Zaarah Herbals Rasayan Churan, Zaarah Herbals Gurmar Powder, Zaarah Herbals Vasaka Powder, and Zaarah Herbals Bhringraj Powder to the consumer/user level because it has the potential to be contaminated with elevated levels of lead and arsenic.
Consumption of inorganic arsenic has been associated with cancer, skin lesions, cardiovascular disease, and diabetes in humans. Inorganic arsenic exposure during fetal development, infancy, and childhood may contribute to neurodevelopment effects, as well as increase lifetime cancer risk.
Zaarah Herbals products were distributed to retailers located in New York, New Jersey, Connecticut and California between Dec. 20, 2024 and Jan. 7, 2025.
The recalled products are packaged in clear 100g (3.5oz) jars with a gold lids. The name of the product is prominently displayed on the front of the jars.
The following codes are included in the recall:
BRAND
Product Description
Batch No.
Mfd. Date
UPC
ZAARAH HERBALS
Bhringraj Powder
BJ 04
July/2022
6 35028 99973 1
ZAARAH HERBALS
Gurmar Powder
GD 04
July/2022
6 35028 99969 4
ZAARAH HERBALS
Vasaka Powder
VK 04
July/2022
6 35028 99967 0
ZAARAH HERBALS
Rasayan Churan
RY 04
July/2022
6 35028 99966 3
All Codes can be found on the back panel of the bottles. No illnesses have been reported to date.
The recall is the result of an analysis conducted by the Connecticut Department of Consumer Protection; Food & Standards Division that revealed the product contained elevated levels of lead and inorganic arsenic.
Consumers who have purchased these products should not consume them and can return to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-516-7606 Monday through Friday from 10:00 am to 6:00 pm EDT.
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Triumph recalls 2025 speed twin motorcycles over rear lighting safety concerns
Triumph recalls Speed Twin 2025 for rear lighting compliance issue
March 8, 2025A voluntary recall has been issued for 2025 Triumph Speed Twin motorcycles due to a possible issue with the rear lighting system that might not meet federal safety standards. Internal testing identified potential noncompliance with Federal Motor Vehicle Safety Standard (FMVSS) No. 108, prompting the company to take action.
An estimated 2,000 units are affected by this notice. These motorcycles were sold at authorized Triumph dealerships across the United States, with sales beginning in early 2025. While no injuries have been reported, the company is removing unsold inventory from dealerships and is coordinating with regulatory agencies to address the concern.
What to look for?
Product name and description
- Motorcycle model and year: 2025 Triumph Speed Twin
- Design features: Standard Speed Twin branding on the side, black and chrome finishes, and distinctive twin-pod instrumentation
Identifiers
- Batch/lot number: Located on a label under the seat
- VIN: Stamped on the steering head and listed on the certification label
- Date of manufacture: Displayed on the same certification label along with the VIN
Affected purchase locations and dates
- Authorized dealerships: Sold through Triumph retailers throughout the United States
- Sale timeframe: Distributed from January 2025 to the date of this announcement
What should buyers do?
Product return or disposal
- Stop riding the motorcycle: Contact the nearest Triumph dealership for further instructions
- Do not attempt repairs at home: Factory-authorized technicians will handle necessary inspections and repairs
Refunds, replacements, or repairs
- All repairs covered: The company will provide free repair service to correct the lighting issue
- How to claim: Call customer support at 1-800-555-1234 or email support@triumphmotorcycles.com
- Customer service hours: Monday-Friday, 9 AM - 5 PM EST
Health and safety advice
No immediate health concerns have been reported. If any rider experiences reduced visibility or is involved in an incident, consulting a healthcare professional is advised.
Sources
- View FMVSS 108 regulations
- Check for open recalls
- Read about a previous Triumph recall
- See details on a brake disc recall
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Jayco recalls 2025 Eagle HT fifth wheels for incorrect axle weight label
Incorrect axle label prompts recall of 2025 Jayco Eagle HT models
March 8, 2025A recall has been issued for 2025 Jayco Eagle HT fifth wheels due to incorrect information on the vehicle certification label. This action has been coordinated with the National Highway Traffic Safety Administration (NHTSA). The issue involves an inaccurate Gross Axle Weight Rating (GAWR) noted on the label, which does not meet the requirements of 49 CFR Part 567. Internal reviews led to the discovery of this labeling error.
Approximately 49 units are estimated to be affected, and they were distributed nationwide through authorized Jayco dealers. The company has taken action to correct the labeling by contacting owners and arranging for proper remediation.
What to look for?
Product name and description
- Product Name and Variations: 2025 Jayco Eagle HT fifth wheels
- Physical Characteristics: These fifth wheels typically feature Jaycos logo and branding on the exterior. Packaging details (e.g., model documentation) accompany the vehicle purchase.
Identifiers
- Label Information: The certification label is located on the drivers side front corner of the fifth wheel
- Incorrect GAWR Noted: The inaccurate value is printed on this label
- Jayco Recall Number: 9901613
- NHTSA Campaign Number: 25V-042
Affected purchase locations and dates
- Purchase Locations: Sold through authorized Jayco dealerships across the United States
- Timeframe: Distributed to consumers within the 2025 model year release period
What should buyers do?
Disposal or return
- These vehicles should not be disposed of. Owners are encouraged to contact Jayco or return to a dealer for corrective labeling
- No hazardous materials are involved, so there is no need for special disposal methods
Refunds, replacements, or repairs
- Remedial Label Replacement: Jayco will provide an updated certification label at no charge
- Contact Information: Call Jayco customer service at (800) 283-8267
- Customer Service Hours: Monday-Friday, 9 AM - 5 PM EST
- How to Proceed: Owners can request a corrected label to be mailed or schedule a service appointment at an authorized dealer
Health and safety advice
An incorrect GAWR may lead to overloading the vehicle, which can increase the risk of accidents. Owners should check if they have experienced any handling issues or near-accidents. If personal injury or property damage has occurred, contact a medical or legal professional for guidance.
Sources
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Taylor Water Technologies is recalling phosphate reagent bottles sold with test kits
The bottle dont have child-resistant tops and pose a chemical burn hazard
March 7, 2025Taylor Water Technologies has issued a recall for 10,000 phosphate reagent bottles sold with test kits because they violate federal child-resistant packaging regulations. The Consumer Product Safety Commission said the bottles lack child-resistant caps and could pose a chemical burn hazard to children.
No incidents have been reported.
This recall involves the replacement reagent #1 bottles sold with Taylor Phosphate Test Kits #K-1106 and also sold separately. The kits are used to test the level of phosphate in water for pools, spas and aquariums. The water testing kits are labeled with the brand name Taylor, the kit name Phosphate Test and part number K-1106.
The bottle in the kit that contains sulfuric acid is labeled with the brand name Taylor, product name Phosphate Reagent #1, part number R-0980 and A Size: 22 mL (.75 oz). The replacement reagent bottle that is sold separately has the same label. Phosphate Reagent #1 has a shelf-life of 24 months.
The test kits were sold Online at www.taylortechnologies.com and other websites and in pool and aquarium stores nationwide from August 2022 through August 2024 for about $13 for the reagent bottles and $56 for the kits that include the reagent bottles.
What to do
Consumers should stop using the recalled Phosphate Reagent #1 bottles immediately, place them in a safe and secure location away from the reach of children and contact Taylor Water Technologies for information on how to properly dispose of the recalled bottle and obtain a free replacement bottle.
Only unexpired Phosphate Reagent #1 bottles are included in this recall and eligible for the free replacement. Taylor Water Technologies is contacting all known purchasers directly.
Consumers may contact Taylor Water Technologies at 800-837-8548 from 8 a.m. to 5 p.m. ET Monday through Friday, via the online contact form at https://www.taylortechnologies.com/en/content/contact-customer-service, or by visiting https://www.taylortechnologies.com and clicking on Recall Information under the Resource Center tab at the top of the page for more information or at https://www.taylortechnologies.com/en/content/recall-information.Sign up below for The Daily Consumer, our newsletter on the latest consumer news, including recalls, scams, lawsuits and more.
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Children’s bathrobes sold on Amazon recalled due to burn hazard
Lolanta bathrobes violate federal flammability regulations
March 6, 2025More than 5,000 Lolanta childrens bathrobes are being recalled because they are in violation of federal flammability standards. The bathrobes were sold exclusively on Amazon from November 2021 through November 2024 for about $29.
This recall involves 100% polyester hooded dinosaur childrens bathrobes. The flannel bathrobes are green and have attached belts and patch pockets. The size, manufacturer information and care instructions are printed on sewn-in labels inside the left inseam of the robes. They were sold in sizes 2-3 years, 3-5 years, 6-8 years, and 8-10 years.
What to do
Consumers should immediately stop using the recalled bathrobes, take them away from children, and contact Nanchang Zhongcangjishi E-commerce for a full refund. Consumers will be asked to destroy the garments by cutting them in half and emailing a photo of the destroyed garment to business@lolanta.com.
Upon receipt of the photo, consumers will be issued a full refund of the purchase price. Amazon and Nanchang Zhongcangjishi E-commerce are contacting all known purchasers directly.
Consumers may contact Nanchang Zhongcangjishi E-commerce by email at business@lolanta.com, or online at https://lolanta.com/recalls or https://lolanta.com/ and click on Product Recall at the top of the page for more information.
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Luv n' care recalls Nuby stroller fans due to laceration injury hazard
The company has received six reports of injuries to children
March 6, 2025Luv n' care has issued a recall of about 33,600 Nuby stroller fans due to a laceration injury hazard. The stroller fans housing allows consumers fingers to contact the fans blade, posing a laceration injury hazard to small children.
Luv n' care has received seven reports of childrens fingers accessing the fan blade, resulting in six laceration injuries.
This recall involves Nuby Stroller Fans with three speeds, adjustable tripod legs and a rechargeable USB port used for babies and toddlers. The flexible tripod legs wrap around the bar of the stroller.
The plastic fans are black with the Nuby brand name printed on the center on the front of the fan. The lot number N8K10X and model number 25138 are printed on a white label on the back center of the fan.
The fans were sold at Baby Express, Burlington Coat Factory, Target, and Unique Photo stores nationwide, and online at Amazon.com and us.nuby.com from May 2024 through June 2024 for about $15.
What to do
Consumers should stop using the stroller fan immediately and contact Luv n care for information on how to return the product to obtain a free replacement. Luv n care is contacting all known purchasers directly.
Consumers may contact Luv n' care at 800-588-6227 from 8 a.m. to 5 p.m. CT Monday through Friday, email customers@nuby.com, or https://us.nuby.com/pages/fanrecall or online at www.nuby.us.com and click on Important Safety Information for more information.
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Ford recalls 2022 Maverick trucks again for unresolved brake light issue
Second recall issued for 2022 Mavericks due to persistent brake light flaw
March 4, 2025A voluntary recall has been issued for certain 2022 Ford Maverick trucks. These vehicles were previously repaired under recall reference 22V-730. The recall addresses a software issue within the Antilock Brake System (ABS) module that may cause brake lights to turn on unexpectedly, even when the brakes are not applied.
This condition was identified following reports that the earlier service action did not fully resolve the risk. The affected vehicles were sold across the United States through authorized Ford dealerships, and the exact number of units involved is currently unavailable. Ford is working with dealerships to reprogram the ABS module and notify owners, at no cost to those affected.
What to look for?
Product name and description:
- 2022 Ford Maverick trucks
- Compact pickup trucks bearing the official Ford logo and Maverick branding elements
Identifiers:
- Recall affects vehicles previously repaired under recall 22V-730
- The Vehicle Identification Number (VIN) can help confirm involvement in the new recall
- Owners can verify recall status by checking documentation provided by Ford or consulting online recall resources
Affected purchase locations and dates:
- Sold at authorized Ford dealerships throughout the United States
- Originally purchased between 2022 and the present date if serviced under the earlier recall
What should buyers do?
Next steps:
- Contact an authorized Ford dealership for free reprogramming of the ABS module
- Refrain from ignoring warning lights or other signs of brake system malfunction
Refunds, replacements, or repairs:
- Repairs are available at no cost
- For details on claiming a cost-free repair, call Fords customer service or visit Fords online recall lookup tool
- Official support is available Monday-Friday, 9 AM - 5 PM EST
Health and safety advice:
- If brake lights illuminate unexpectedly, exercise caution when driving to avoid confusion for other drivers
- Any relevant symptoms (such as potential rear-end near-misses) should be reported to a dealership
- Seek advice from a qualified automotive technician if any safety concerns arise
Sources
- NHTSA official recall interpretations
- Ford recall lookup tool
- FMVSS 108 regulation text
- Previous recall details
- Related news report
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